Join a dynamic pharmaceutical manufacturing environment where you will take ownership of Computerised Systems Validation and IT infrastructure qualification across the site. This is a rare opportunity to work independently, apply your expertise broadly and influence how compliant digital systems are governed throughout their lifecycle.

You will play a central role in modernising and digitising CSV practices, strengthening risk-based assurance and helping shape a future-ready validation framework. Working closely with Quality, IT, Engineering and system owners, you will have the scope to drive meaningful improvement while ensuring systems, infrastructure and electronic records remain compliant, reliable and fit for intended use.